Last synced on 14 November 2025 at 11:06 pm

NEEDLE GUARD(TM)

Page Type
Cleared 510(K)
510(k) Number
K890473
510(k) Type
Traditional
Applicant
MARTECH MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/1989
Days to Decision
62 days

NEEDLE GUARD(TM)

Page Type
Cleared 510(K)
510(k) Number
K890473
510(k) Type
Traditional
Applicant
MARTECH MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/1989
Days to Decision
62 days